INTEGRAL REVISION HIP SYSTEM 166023

GUDID 00880304257900

Coated hip femur prosthesis, modular

Primary Device ID	00880304257900
NIH Device Record Key	f34e6ce3-3b26-4589-ba64-49ab3f42dd3a
Commercial Distribution Status	In Commercial Distribution
Brand Name	INTEGRAL REVISION HIP SYSTEM
Version Model Number	166023
Catalog Number	166023
Company DUNS	129278169
Company Name	Biomet Orthopedics, LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Phone	+1(800)348-9500
Email	customerservice@zimmerbiomet.com

Device Size Text, specify

Device Issuing Agency	Device ID
GS1	00880304257900 [Primary]

MEH	Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate

Steralize Prior To Use	false
Device Is Sterile	true